Variant report

Variant	rs4683324
Chromosome Location	chr3:47251284-47251285
allele	C/T
Outlinks	Ensembl UCSC

Chromatin state
Related regulatory elements
Target genes
Other information

No.	Distal block	Cell Line	Cell type	Cell Stage
1	chr3:47246768..47248949-chr3:47249706..47251385,2	K562	blood:

Extended variants
information (count: 64 )
Associated
traits (count: 2 )

rSNPs within LD-proxies of this variant (count:58)

rs_ID	r²[population]
rs11130114	0.81[AMR][1000 genomes];0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs11130115	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11130123	0.82[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11130124	0.81[EUR][1000 genomes];0.80[ASN][1000 genomes]
rs11708451	0.91[EUR][1000 genomes];0.90[ASN][1000 genomes]
rs11712716	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11714282	0.81[EUR][1000 genomes];0.81[ASN][1000 genomes]
rs11714373	0.82[EUR][1000 genomes]
rs11716539	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs11718795	0.90[EUR][1000 genomes];0.92[ASN][1000 genomes]
rs11719306	0.89[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs11719738	0.83[EUR][1000 genomes]
rs11920354	0.84[EUR][1000 genomes]
rs11925560	0.85[EUR][1000 genomes]
rs12488225	0.89[AMR][1000 genomes];0.92[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs12489211	0.88[EUR][1000 genomes];0.91[ASN][1000 genomes]
rs12493425	0.83[EUR][1000 genomes]
rs12629262	0.91[EUR][1000 genomes];0.87[ASN][1000 genomes]
rs12635619	0.81[AMR][1000 genomes];0.93[EUR][1000 genomes];0.94[ASN][1000 genomes]
rs13061071	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs13062022	0.90[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13063250	0.90[EUR][1000 genomes];0.93[ASN][1000 genomes]
rs13078131	0.81[AMR][1000 genomes];0.82[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs13084117	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs13094438	0.81[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs13094672	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs13098228	0.87[EUR][1000 genomes];0.86[ASN][1000 genomes]
rs1466740	0.91[EUR][1000 genomes]
rs1466741	0.91[EUR][1000 genomes]
rs1811652	0.83[EUR][1000 genomes]
rs2088135	0.81[EUR][1000 genomes]
rs2132173	0.88[AMR][1000 genomes];0.99[EUR][1000 genomes];1.00[ASN][1000 genomes]
rs2276853	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs2276854	0.92[AMR][1000 genomes];0.88[EUR][1000 genomes];0.96[ASN][1000 genomes]
rs4682852	0.83[AMR][1000 genomes];0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs4683320	0.90[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs4683326	0.80[ASN][1000 genomes]
rs56250009	0.81[EUR][1000 genomes]
rs57756484	0.85[EUR][1000 genomes]
rs58956475	0.82[EUR][1000 genomes]
rs62246451	0.83[EUR][1000 genomes]
rs62246455	0.84[EUR][1000 genomes]
rs6442059	0.83[EUR][1000 genomes]
rs6766230	0.83[EUR][1000 genomes]
rs6767907	0.82[EUR][1000 genomes]
rs6772670	0.91[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs6773521	0.84[EUR][1000 genomes]
rs6781941	0.82[EUR][1000 genomes]
rs6785790	0.88[EUR][1000 genomes];0.88[ASN][1000 genomes]
rs6791062	0.81[EUR][1000 genomes]
rs6791842	0.90[AMR][1000 genomes];0.89[EUR][1000 genomes];0.95[ASN][1000 genomes]
rs7615323	0.81[AMR][1000 genomes];0.87[EUR][1000 genomes];0.89[ASN][1000 genomes]
rs7621911	0.83[EUR][1000 genomes];0.84[ASN][1000 genomes]
rs7632501	0.83[EUR][1000 genomes]
rs7636423	0.80[ASN][1000 genomes]
rs9818382	0.83[EUR][1000 genomes]
rs9821119	0.83[EUR][1000 genomes]
rs9837343	0.83[EUR][1000 genomes]

Variant overlapped rSNPs/rCNVs (count:6 , 50 per page) page: 1

No.	Variant name	Chromosome position	Chromatin state	Related regulatory elements	Target genes	Extended variants	Associated traits
1	nsv876756	chr3:47002931-47586514	Strong transcription Enhancers Weak transcription Transcr. at gene 5' and 3' Active TSS Genic enhancers Flanking Active TSS ZNF genes & repeats Flanking Bivalent TSS/Enh Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA miRNA target site	79 gene(s)	inside rSNPs	diseases
2	nsv1007714	chr3:47084387-47331570	Transcr. at gene 5' and 3' Weak transcription Enhancers Genic enhancers Active TSS Strong transcription Flanking Active TSS Flanking Bivalent TSS/Enh ZNF genes & repeats Bivalent Enhancer Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	35 gene(s)	inside rSNPs	diseases
3	nsv590211	chr3:47189485-47256057	Flanking Active TSS Active TSS Enhancers Weak transcription Strong transcription Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	13 gene(s)	inside rSNPs	diseases
4	nsv1014457	chr3:47222292-47335175	Enhancers Strong transcription Weak transcription Flanking Active TSS Active TSS Transcr. at gene 5' and 3' Genic enhancers Flanking Bivalent TSS/Enh Bivalent Enhancer ZNF genes & repeats Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
5	nsv536560	chr3:47222292-47335175	Weak transcription Flanking Active TSS Active TSS Enhancers Flanking Bivalent TSS/Enh Strong transcription Bivalent Enhancer Genic enhancers ZNF genes & repeats Transcr. at gene 5' and 3' Bivalent/Poised TSS	TF binding region CpG island Chromatin interactive region lncRNA	24 gene(s)	inside rSNPs	diseases
6	nsv238095	chr3:47248230-47253427	Weak transcription Enhancers	Chromatin interactive region lncRNA	n/a	inside rSNPs	diseases

mRNA abundance (count:2)

SNP	Gene	Cis/trans	Tissue	Source
rs4683324	SETD2	Cis_1M	lymphoblastoid	RTeQTL
rs4683324	KLHL18	Cis_1M	lymphoblastoid	RTeQTL

Chromatin state (count:10 , 50 per page) page: 1

No.	Chromosome Location	Chromatin state	Cell line	Tissue
1	chr3:47207000-47253800	Weak transcription	Aorta	Aorta
2	chr3:47208200-47256400	Weak transcription	Brain Cingulate Gyrus	brain
3	chr3:47208200-47276600	Weak transcription	Foreskin Fibroblast Primary Cells skin02	Skin
4	chr3:47223400-47256600	Weak transcription	Brain Inferior Temporal Lobe	brain
5	chr3:47223800-47252600	Weak transcription	Fetal Muscle Leg	muscle
6	chr3:47223800-47269200	Weak transcription	Fetal Muscle Trunk	muscle
7	chr3:47236200-47256800	Weak transcription	hESC Derived CD184+ Endoderm Cultured Cells	ES cell derived
8	chr3:47238400-47256400	Weak transcription	Right Atrium	heart
9	chr3:47245400-47266600	Weak transcription	hESC Derived CD56+ Mesoderm Cultured Cells	ES cell derived
10	chr3:47247000-47269400	Weak transcription	iPS DF 19.11 Cell Line	embryonic stem cell

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